Application | Comment | Organism |
---|---|---|
drug development | CDA is a target for development of specific enzyme inhibitors with potential anti-proliferative activity on cell growth of Mycobacterium tuberculosis, the major causative agent of tuberculosis | Mycobacterium tuberculosis |
Crystallization (Comment) | Organism |
---|---|
purified CDA in complex with uridine and deoxyuridine, hanging drop vapor diffusion method, 0.002 ml of 12 mg/ml protein in 20 mM Tris-HCl pH 7.5 is mixed with 0.002 ml of reservoir solution containing 0.1 M HEPES, pH 7.5 and 4.3 M sodium chloride, ligands uridine and deoxyuridine are added by soaking method, X-ray diffractiuon structure determination and analysis at 2.4 and 1.9 A resolution,molecular dynamics simulation, structure modeling | Mycobacterium tuberculosis |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Mycobacterium tuberculosis | P9WPH3 | - |
- |
Mycobacterium tuberculosis H37Rv | P9WPH3 | - |
- |
Subunits | Comment | Organism |
---|---|---|
tetramer | - |
Mycobacterium tuberculosis |
Synonyms | Comment | Organism |
---|---|---|
CDA | - |
Mycobacterium tuberculosis |
General Information | Comment | Organism |
---|---|---|
metabolism | cytidine deaminase is a key enzyme in the pyrimidine salvage pathway | Mycobacterium tuberculosis |
physiological function | cytidine amidase is involved in the hydrolytic deamination of cytidine or 2'-deoxycytidine to uridine or 2'-deoxyuridine, determination of the protein-ligand recognition process, respectively | Mycobacterium tuberculosis |